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Gymnomitrion obtusum

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID6440520d4768f758298200
Scientific name Gymnomitrion obtusum
Authority (Lindb.) Pearson
First published in J. Bot. 18: 337

Description Top

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Synonyms Top

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Common names Top

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Language Common/alternative name
Czech skulinatka tupá
Welsh baruglys gwyn
Finnish etelänhopeasammal
Swedish trubbfrostmossa

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001207843
USDA Plants GYOB
Tropicos 35208748
INPN 6434
The Plant List tro-35208748
Open Tree Of Life 3855949
NCBI Taxonomy 1527723
NBN Atlas NHMSYS0000310000
Nature Serve 2.125508
iNaturalist 163459
GBIF 5286355
EOL 604327

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
The distribution and evolution of fungal symbioses in ancient lineages of land plants Rimington WR, Duckett JG, Field KJ, Bidartondo MI, Pressel S Mycorrhiza 04-Mar-2020
PMCID:PMC7062687
doi:10.1007/s00572-020-00938-y
PMID:32130512
Gymnomitrol and related sesquiterpenoids from the liverwort Gymnomitrion obtusum(Lindb) pears (Hepaticae). A novel tricyclic skeleton Joseph D. Connolly, Alexander E. Harding, Ian M. S. Thornton Royal Society of Chemistry (RSC) 23-Apr-2004
doi:10.1039/P19740002487
Gymnomitrol, a novel tricyclic sesquiterpenoid from Gymnomitrion obtusum(Lindb) Pears (hepaticae) J. D. Connolly, A. E. Harding, I. M. S. Thornton Royal Society of Chemistry (RSC) 29-Mar-2004
doi:10.1039/C39720001320

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
4,8-Methanoazulene, decahydro-3a,4,8a-trimethyl-7-methylene-, (3aR,4R,8R,8aS)-rel- 524194 Click to see CC12CCC(=C)C(C1)C3(C2(CCC3)C)C 204.35 unknown https://doi.org/10.1039/C39720001320
beta-Barbatene 14109421 Click to see CC12CCC(=C)C(C1)C3(C2(CCC3)C)C 204.35 unknown https://doi.org/10.1039/P19740002487
https://doi.org/10.1039/C39720001320
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
(1,2,6-Trimethyl-8-methylidene-11-tricyclo[5.3.1.02,6]undecanyl) acetate 162857607 Click to see CC(=O)OC1C2C(=C)CCC1(C3(C2(CCC3)C)C)C 262.40 unknown https://doi.org/10.1039/C39720001320
[(1S,2S,6S,7R,11S)-1,2,6-trimethyl-8-methylidene-11-tricyclo[5.3.1.02,6]undecanyl] acetate 162857608 Click to see CC(=O)OC1C2C(=C)CCC1(C3(C2(CCC3)C)C)C 262.40 unknown https://doi.org/10.1039/C39720001320
[(1S,2S,6S,7S,11S)-8-(hydroxymethyl)-1,2,6-trimethyl-11-tricyclo[5.3.1.02,6]undec-8-enyl] acetate 162935541 Click to see CC(=O)OC1C2C(=CCC1(C3(C2(CCC3)C)C)C)CO 278.40 unknown https://doi.org/10.1039/P19740002487
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
(11'-Acetyloxy-2',6',7'-trimethylspiro[oxirane-2,10'-tricyclo[5.3.1.02,6]undecane]-3'-yl) acetate 162925201 Click to see CC(=O)OC1CCC2(C1(C3C(C2(CCC34CO4)C)OC(=O)C)C)C 336.40 unknown https://doi.org/10.1039/C39720001320
[(1'R,2R,2'S,3'S,6'R,7'S,11'S)-11'-acetyloxy-2',6',7'-trimethylspiro[oxirane-2,10'-tricyclo[5.3.1.02,6]undecane]-3'-yl] acetate 162925202 Click to see CC(=O)OC1CCC2(C1(C3C(C2(CCC34CO4)C)OC(=O)C)C)C 336.40 unknown https://doi.org/10.1039/C39720001320
[(1R,2S,3S,6R,7S,11S)-11-acetyloxy-10-(hydroxymethyl)-2,6,7-trimethyl-3-tricyclo[5.3.1.02,6]undec-9-enyl] acetate 162981757 Click to see CC(=O)OC1CCC2(C1(C3C(C2(CC=C3CO)C)OC(=O)C)C)C 336.40 unknown https://doi.org/10.1039/P19740002487
[(1R,2S,3S,6R,7S,11S)-11-acetyloxy-2,6,7-trimethyl-10-methylidene-3-tricyclo[5.3.1.02,6]undecanyl] acetate 162925965 Click to see CC(=O)OC1CCC2(C1(C3C(C2(CCC3=C)C)OC(=O)C)C)C 320.40 unknown https://doi.org/10.1039/P19740002487
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
(1S,2S,6S,7R,11R)-1,2,6-trimethyl-8-methylidenetricyclo[5.3.1.02,6]undecan-11-ol 14109430 Click to see CC12CCCC1(C3(CCC(=C)C2C3O)C)C 220.35 unknown https://doi.org/10.1039/P19740002487
(1S,2S,6S,7R,11S)-1,2,6-trimethyl-8-methylidenetricyclo[5.3.1.02,6]undecan-11-ol 14109432 Click to see CC12CCCC1(C3(CCC(=C)C2C3O)C)C 220.35 unknown https://doi.org/10.1039/C39720001320
1,2,6-Trimethyl-8-methylidenetricyclo[5.3.1.02,6]undecan-11-ol 14109431 Click to see CC12CCCC1(C3(CCC(=C)C2C3O)C)C 220.35 unknown https://doi.org/10.1039/C39720001320

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